Endocrinology and Hormones(内分泌和激素)

Endocrinology and Hormones
The endocrine system is an information signaling system that coordinates most bodily functions. It senses environmental changes and secretes corresponding hormones to coordinate metabolism, maintain homeostasis, and regulate growth and development.read more
Products for Endocrinology and Hormones
- 5-alpha Reductase(8)
- Androgen Receptor(149)
- Aromatase(12)
- CRTH2(2)
- Estrogen/progestogen Receptor(157)
- GnRH(27)
- Opioid Receptor(148)
- RAAS(7)
- Thyroid hormone Receptor(65)
- TRH(1)
- Smoothened Receptors(3)
- ROR/RAR/RXR(89)
- FXR & LXR(77)
- Glucocorticoids & Mineralocorticoids(65)
- GPR(1)
- Androgen/Estrogen Receptor Modulators(1)
- Cat.No. 产品名称 Information
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GC46892
ATRA-BA Hybrid
A prodrug form of all-trans retinoic acid and butyric acid
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GC46860
AP-238 (hydrochloride)
2,6-dimethyl Propionyl AP-237
A neuropeptide with diverse biological activities -
GC46859
Antide (acetate)
N-((4R,7R,10R,13S,16S,19R)-19-(((S)-1-(((S)-1-((S)-2-((R)-1-氨基-1-氧代丙烷-2-基)氨基甲酰基)吡咯烷-1-基)-6-(异丙基氨基)-1-氧代己基-2-基)氨基)-4-甲基-1-氧代戊烷-2-基)氨基甲酰基)-7-(4-氯苄基)-13-(羟甲基)-4-(萘-2-基甲基)-16-(4-(烟酰胺基)丁基)-2,5,8,11,14,17-六氧代-10-(吡啶-3-基甲基)-3,6,9,12,15,18-六氮杂二十三烷-23-基)烟酰胺乙酸盐
A GnRHR antagonist -
GC46856
Angiotensin II (5-8) (human, rat, mouse) (trifluoroacetate salt)
Angiotensin (5-8)
An endogenous angiotensin II fragment -
GC46854
Anastrozole-d12
ZD1033-d12
An internal standard for the quantification of anastrozole -
GC46827
Aldosterone 21-sulfate (sodium salt)
Aldosterone 21-sulphate
A metabolite of aldosterone -
GC46798
Adapalene-d3
阿达帕林 d3
An internal standard for the quantification of adapalene -
GC46777
AC-262536
4-(3-内型-羟基-8-氮杂双环[3.2.1]辛烷-8-基)萘-1-甲腈
A selective androgen receptor modulator
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GC46775
Abiraterone Acetate-d4
CB7630-d4
醋酸阿比特龙-d4 (CB7630-d4) 是氘标记的醋酸阿比特龙。醋酸阿比特龙 (CB7630) 是一种口服的、有效的、选择性的、不可逆的 CYP17A1 抑制剂,具有抗雄激素活性。醋酸阿比特龙是阿比特龙 (CB7598) 的前药形式。 -
GC46768
Abaloparatide (acetate)
BA 058, BIM 44058
A synthetic derivative of PTHrP and an agonist of PTHR1 -
GC46754
9(S)-HETE-d8
9(S)-Hydroxyeicosatetraenoic Acid-d8
A neuropeptide with diverse biological activities -
GC46740
7β,27-dihydroxy Cholesterol
7β,27-DHC
An oxysterol and agonist of RORγ and RORγt -
GC46526
21-Deoxycortisol
脱氧皮质醇
A corticosteroid metabolite of 17-hydroxyprogesterone -
GC46471
17β-hydroxy Exemestane-d3
A neuropeptide with diverse biological activities
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GC46470
17β-Estradiol-d2
BETA-雌二醇-D2,β-Estradiol-d2; 17β-Estradiol-d2; 17β-Oestradiol-d2
An internal standard for the quantification of 17β-estradiol -
GC46456
16α-Hydroxyetiocholanolone
A metabolite of 16α-DHEA and androstenedione
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GC46361
[Leu15]-Gastrin I amide (human) (trifluoroacetate salt)
15-Leu-Gastrin-17
胃泌素是一种胃肠道激素,其结构类似于羧基末端氨基酸。 -
GC46336
(E)-Guggulsterone
孕二烯二酮,(E)-Guggulsterone
A farnesoid X receptor antagonist -
GC46313
(±)-α-Tocopherol Acetate-d3
all-rac-α-Tocopherol Acetate-d3, DL-α-Tocopherol Acetate-d3, DL-Vitamin E Acetate-d3
A neuropeptide with diverse biological activities -
GC61267
SAR439859
SAR439859
Amcenestrant (SAR439859, compound 43d) is an orally available and nonsteroidal selective estrogen receptor degrader (SERD) with potential antineoplastic activity. SAR439859 is a potent estrogen receptor (ER) antagonist with EC50 of 0.2 nM for ERα degradation. -
GC61010
L-Thyroxine sodium
Levothyroxine sodium; T4 sodium
A synthetic form of thyroxine -
GC61003
Loperamide D6 hydrochloride
4-[4-(4-氯苯基)-4-羟基哌啶-1-基]-2,2-二苯基-N,N-二(三氘甲基)丁酰胺盐酸盐,R-18553-d6 hydrochloride
LoperamideD6hydrochloride(R-18553D6hydrochloride)是Loperamidehydrochloride的氘代化合物。Loperamidehydrochloride是一种阿片受体(opioidreceptor)的激动剂,可用于腹泻的研究。 -
GC60857
Frakefamide TFA
FrakefamideTFA具有有效的止痛作用,是选择性的μ受体的外围激动剂。Frakefamide不能透过血脑屏障,进入中枢神经系统。
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GC60842
Finerenone
非奈利酮,BAY 94-8862
非奈利酮(Finerenone;BAY 94-8862)是第三代选择性、具有口服活性的、非甾体类盐皮质激素受体 (MR)拮抗剂,IC50为18 nM。 -
GC60731
CTOP TFA
CTOPTFA是一种多肽,可以作为μ-opioidreceptor的拮抗剂。
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GC60730
CTAP TFA
CTAPTFA是一种强效、高选择性的脑渗透类阿片受体(μopioidreceptor)拮抗剂(IC50=3.5nM),对δopioid受体(IC50=4500nM)和生长抑素受体具有超过1200倍的选择性。CTAPTFA可用于L-多巴胺诱导的运动障碍(LID)的研究。
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GC60725
Cortisone
17α-hydroxy-11-Dehydrocorticosterone, Kendall’s Compound E, 4-Pregnene-17α,21-diol-3,11,20-trione, Reichstein’s Substance Fa
Cortisone(17-Hydroxy-11-dehydrocorticosterone)是一种用于研究感染或过敏的激素药物。 -
GC60589
Apalutamide D4
ARN-509-d4
ApalutamideD4(ARN-509D4)是Apalutamide的一种氘代化合物。Apalutamide是有效,竞争性的雄激素受体(AR)拮抗剂,IC50为16nM。 -
GC60391
β-Casomorphin, bovine TFA
β-Casomorphin-7 (bovine) (TFA); Bovine β-casomorphin-7 TFA
β-casomorphin, bovine TFA (β-Casomorphin-7 (bovine) TFA) 是阿片 (opioid) 活性的多肽,与阿片受体结合的 IC50 值为 14 μM。 -
GC60076
Bigelovin
锦菊素
Bigelovin是可从海百合中分离得到的一种倍半萜内酯,是选择性的视黄素X受体α(retinoidXreceptorα)的激动剂。Bigelovin可通过诱导凋亡和自噬来发挥抗肿瘤活性。Bigelovin通过抑制ROS的生成来调节mTOR信号通路。 -
GC39619
SB-612111
(5S,7S)-7-[[4-(2,6-二氯苯基)-1-哌啶基]甲基]-6,7,8,9-四氢-1-甲基-5H-苯并环庚烯-5-醇
SB-612111 是一种新型高效的人阿片受体孤儿受体 (ORL-1) 拮抗剂,对 hORL-1 具有较高的亲和力 (Ki=0.33 nM)。SB-612111 对 μ-,κ- 和 δ-receptor 的 Ki 值分别为 57.6 nM,160.5 nM 和 2109 nM。SB-612111 能有效拮抗 Nociceptin 在急性疼痛模型中的造成的痛觉作用。 -
GC39584
AGN194204
IRX4204; NRX194204; VTP 194204
AGN194204 (IRX4204) 是一种具有口服活性的,选择性 RXR 激动剂,对 RXRα,RXRβ 和 RXRγ 的 Kd 值分别为 0.4 nM,3.6 nM 和 3.8 nM,EC50 分别为 0.2 nM,0.8 nM 和 0.08 nM。AGN194204 对 RAR 无活性,并具有抗炎和抗癌作用。 -
GC39535
Yamogenin
雅姆皂甙元; Neodiosgenin
A steroidal sapogenin with diverse biological activities -
GC39451
Testosterone (propionate)
丙酸睾丸素
An Analytical Reference Standard -
GC50558
TAN 452
TAN 452 是一种具有口服活性的选择性外周作用 δ-阿片受体 (DOR) 拮抗剂,Ki 为 0.47nM,Kb 为 0.21nM。
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GC50491
PF 04449913 maleate
A Smo antagonist
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GC50438
SAG dihydrochloride
An agonist of Smoothened
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GC50279
MK 386
Potent, selective human type 1 5α-reductase inhibitor
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GC50201
IHR 1
IHR 1 是一种细胞膜不可渗透的 Smo 拮抗剂。
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GC50190
Fenretinide - d4
4-HPR-d4, 4-Hydroxy(phenyl)retinamide-d4, Retinoic Acid p-hydroxyphenylamide-d4
An internal standard for the quantification of fenretinide -
GC50178
DPC AJ1951
A peptide PPR agonist
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GC50091
AC 186
A non-steroidal ERβ agonist
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GC46230
Terrelumamide A
Penilumamide E
A peptide fungal metabolite -
GC46182
Naldemedine
S-297995
Naldemedine (S-297995) 是一种口服有效的 μ-阿片受体拮抗剂 (PAMORA)。 -
GC46104
Butyric Acid-d7
氘代丁酸(D7),Butanoic acid-d7
An internal standard for the quantification of sodium butyrate -
GC46075
5,6-dimethyl-2-Thiouracil
5,6-二甲基--2-硫脲嘧啶
A heterocyclic building block -
GC39193
LY2444296
FP3FBZ
LY2444296 是一种有口服生物活性、高亲和力、选择性的短效的 KOPR 拮抗剂,其 Ki 值为 ~1 nM。LY2444296 具有抗焦虑样的作用。 -
GC45997
Naftifine-d3 (hydrochloride)
盐酸萘替芬 d3 (盐酸盐)
An internal standard for the quantification of naftifine -
GC45969
6β-hydroxy Eplerenone
依普利酮6-BETA-羟基类似物
A major metabolite of eplerenone -
GC38842
Ro 64-6198
Ro 64-6198 是一种有效的,选择性的,非肽,高亲和力,高细胞通透性和脑渗透 N/OFQ 受体 (NOP) 激动剂,EC50 值为 25.6 nM。Ro 64-6198 对 NOP 受体的选择性至少是经典阿片受体的 100 倍。Ro 64-6198 可用于治疗压力和焦虑,成瘾,神经性疼痛,咳嗽和厌食症。